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美沙酮的行为药理学:一种治疗阿片类药物过量和阿片类药物使用障碍的新方法。

Behavioral pharmacology of methocinnamox: A potential new treatment for opioid overdose and opioid use disorder.

机构信息

Department of Pharmacology, University of Texas Health Science Center at San Antonio, TX, United States.

Addiction Research, Treatment, and Training Center of Excellence, University of Texas Health Science Center at San Antonio, TX, United States.

出版信息

J Exp Anal Behav. 2023 Mar;119(2):392-406. doi: 10.1002/jeab.831. Epub 2023 Feb 9.

Abstract

Opioid overdose and opioid use disorder continue to be significant public health challenges despite the availability of effective medications and significant efforts at all levels of society. The emergence of highly potent and efficacious opioids such as fentanyl and its derivatives over the last decade has only exacerbated what was already a substantial problem. Behavioral pharmacology research has proven invaluable for understanding the effects of drugs as well as developing and evaluating pharmacotherapies for disorders involving the central nervous system, including substance abuse disorders. This paper describes a program of research characterizing a potent, selective, and long-lasting mu opioid receptor antagonist, methocinnamox, and evaluating its potential for treating opioid overdose and opioid use disorder. Studies in rodents and nonhuman primates demonstrate that methocinnamox prevents and reverses opioid-induced ventilatory depression and selectively blocks opioid self-administration. This work, taken together with rigorous in vitro and ex vivo studies investigating methocinnamox neuropharmacology, lays a solid foundation for the therapeutic utility of this potentially life-saving medication. Moreover, these studies demonstrate how rigorous behavioral pharmacological studies can be integrated in a broader drug discovery and development research program.

摘要

尽管有有效的药物和社会各层面的大力投入,阿片类药物过量和阿片类使用障碍仍然是重大的公共卫生挑战。在过去十年中,出现了芬太尼及其衍生物等强效有效的阿片类药物,这使得本来就很严重的问题更加恶化。行为药理学研究对于理解药物的作用以及开发和评估涉及中枢神经系统的疾病(包括物质滥用障碍)的药物治疗方法非常有价值。本文描述了一项研究计划,该计划旨在描述一种强效、选择性和长效的μ阿片受体拮抗剂——甲氧基肉桂酰胺,并评估其治疗阿片类药物过量和阿片类使用障碍的潜力。在啮齿动物和非人灵长类动物中的研究表明,甲氧基肉桂酰胺可预防和逆转阿片类药物引起的呼吸抑制,并选择性地阻断阿片类药物的自我给药。这项工作与严格的体外和离体研究相结合,调查了甲氧基肉桂酰胺的神经药理学,为这种潜在的救命药物的治疗用途奠定了坚实的基础。此外,这些研究还表明,严格的行为药理学研究如何可以整合到更广泛的药物发现和开发研究计划中。

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